A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
栏目名称
DOI
10.1097/CM9.0000000000001425
发布时间
2025-04-22
基金项目
This work was supported by grants from the National Natural Science Foundation of China(Nos. 81671237, 81974193)
- 浏览2
- 被引2
- 下载1

相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文